Hartsuiker Edgar
North West Cancer Research Fund Institute, Bangor University, LL57 2UW, Bangor, UK.
Methods Mol Biol. 2011;745:65-77. doi: 10.1007/978-1-61779-129-1_5.
Topoisomerases can release topological stress and resolve DNA catenanes by a DNA strand breakage and re-ligation mechanism. During the lifetime of the DNA break, the topoisomerase remains covalently linked to the DNA and removes itself when the break is re-ligated. While the lifetime of a covalent topoisomerase-DNA complex is usually short, several clinically important cancer drugs kill cancer cells by inhibiting the removal of covalently linked topoisomerases. The topoisomerase-like protein Spo11 is responsible for meiotic double strand break formation. Spo11 is not able to remove itself and is removed by nucleolytic cleavage. This chapter describes a method which allows the reproducible and quantitative detection of proteins covalently bound to the DNA.
拓扑异构酶可通过DNA链断裂和重新连接机制释放拓扑应力并解开DNA连环体。在DNA断裂的存续期间,拓扑异构酶与DNA保持共价连接,并在断裂重新连接时自行脱离。虽然共价拓扑异构酶-DNA复合物的存续期通常较短,但几种临床上重要的抗癌药物通过抑制共价连接的拓扑异构酶的脱离来杀死癌细胞。类拓扑异构酶蛋白Spo11负责减数分裂双链断裂的形成。Spo11无法自行脱离,而是通过核酸裂解被移除。本章介绍了一种可重复且定量检测与DNA共价结合的蛋白质的方法。